Near-haploid B lymphoblastic leukemia with an apparent hyperdiploid karyotype: The critical role of SNP analysis in establishing proper diagnosis

Sarah M. Choi, Peter Papenhausen, Gerald Wertheim, Rebecca L. King

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

Molecular genetic analysis is indispensible in both classification and prognostication of hematopoietic malignancies. The evolution of genetic analysis from conventional cytogenetics to novel genomic technologies has increased our ability to detect subtle and nonconventional mutations in leukemia and lymphoma. Near haploidy, a subtype of hypodiploidy, is a rare entity that carries a particularly poor prognosis in B lymphoblastic leukemia (B-ALL). Near-haploid B-ALL usually quickly evolves by doubling of the chromosome number, creating confusion with the prognostically favorable hyperdiploid B-ALL subtype. Here, we describe a case of B-ALL in which single-nucleotide polymorphism (SNP) microarray analysis was used to identify a hyperdiploid clone that had evolved from a presumptive, near-haploid clone. By conventional methods, this clone may have been easily misinterpreted as a common hyperdiploid clone. Given the extreme prognostic differences of the two clones, this distinction is especially critical to accurately guide therapy. In this case report and brief review, we discuss the role of SNP microarray analysis in the diagnosis and proper subclassification of B-ALL as well as its potential in the identification of genetic therapeutic targets.

Original languageEnglish (US)
Pages (from-to)27-32
Number of pages6
JournalJournal of Hematopathology
Volume7
Issue number1
DOIs
StatePublished - Mar 2014

Keywords

  • ALL
  • B lymphoblastic leukemia
  • Haploid
  • Hypodiploid
  • SNP array

ASJC Scopus subject areas

  • Pathology and Forensic Medicine
  • Histology
  • Hematology

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